Batch Release - 40+ offerte

Novartis Pharma Schweiz

Novartis Pharma Schweiz in Ivrea, Italy, is hiring for a Quality Assurance Officer role. This position involves shift work, including nights and weekends, primarily focused on maintaining compliance with GMP standards within a sterile production environment. Key responsibilities include the validati

Altro

Novartis Pharma Schweiz in Ivrea, Italy, is hiring for a Quality Assurance Officer role. This position involves shift work, including nights and weekends, primarily focused on maintaining compliance with GMP standards within a sterile production environment. Key responsibilities include the validati

Novartis Pharma Schweiz

Novartis Pharma Schweiz in Ivrea, Italy, is hiring for a Quality Assurance Officer role. This position involves shift work, including nights and weekends, primarily focused on maintaining compliance with GMP standards within a sterile production environment. Key responsibilities include the validati

Novartis Italia

Novartis Italia, located in Ivrea, is seeking a QA Officer responsible for quality oversight in GMP activities. This role involves validating production sites, responsible for batch shipment releases, and maintaining quality documentation. The ideal candidate holds a scientific degree and has prior

Novartis ACC

Novartis ACC in Ivrea is searching for a QA Officer responsible for ensuring quality oversight during GMP activities. The role involves working in shifts, including nights and weekends. Key responsibilities include validation of production status, batch release, and documentation management. Ideal c

Altro

Novartis ACC in Ivrea is searching for a QA Officer responsible for ensuring quality oversight during GMP activities. The role involves working in shifts, including nights and weekends. Key responsibilities include validation of production status, batch release, and documentation management. Ideal c

Novartis Acc

Novartis ACC in Ivrea is searching for a QA Officer responsible for ensuring quality oversight during GMP activities. The role involves working in shifts, including nights and weekends. Key responsibilities include validation of production status, batch release, and documentation management. Ideal c

Novartis Italia

Novartis Italia, located in Ivrea, is seeking a QA Officer responsible for quality oversight in GMP activities. This role involves validating production sites, responsible for batch shipment releases, and maintaining quality documentation. The ideal candidate holds a scientific degree and has prior

Novartis Acc

A global healthcare company in Ivrea, Italy, is seeking a Quality Assurance professional to oversee manufacturing processes and ensure compliance with regulations. The role involves assessing and certifying medicinal products, collaborating with various departments, and managing quality-related issu

Novartis

A leading pharmaceutical company in Ivrea is seeking a Qualified Person to independently supervise manufacturing processes and ensure compliance with quality standards. The role involves assessing and releasing manufactured medicinal products, collaborating with various departments, and communicatin

Novartis ACC

A global healthcare company in Ivrea, Italy, is seeking a Quality Assurance professional to oversee manufacturing processes and ensure compliance with regulations. The role involves assessing and certifying medicinal products, collaborating with various departments, and managing quality-related issu

Novartis

A leading pharmaceutical company in Ivrea is seeking a Qualified Person to independently supervise manufacturing processes and ensure compliance with quality standards. The role involves assessing and releasing manufactured medicinal products, collaborating with various departments, and communicatin

Novartis

A leading pharmaceutical company in Ivrea is seeking a Qualified Person to independently supervise manufacturing processes and ensure compliance with quality standards. The role involves assessing and releasing manufactured medicinal products, collaborating with various departments, and communicatin

Novartis ACC

A global healthcare company in Ivrea, Italy, is seeking a Quality Assurance professional to oversee manufacturing processes and ensure compliance with regulations. The role involves assessing and certifying medicinal products, collaborating with various departments, and managing quality-related issu

Novartis ACC

A global healthcare company in Ivrea, Italy, is seeking a Quality Assurance professional to oversee manufacturing processes and ensure compliance with regulations. The role involves assessing and certifying medicinal products, collaborating with various departments, and managing quality-related issu

Novartis

A leading pharmaceutical company in Ivrea is seeking a Qualified Person to independently supervise manufacturing processes and ensure compliance with quality standards. The role involves assessing and releasing manufactured medicinal products, collaborating with various departments, and communicatin

Novartis

A leading pharmaceutical company in Ivrea is seeking a Qualified Person to independently supervise manufacturing processes and ensure compliance with quality standards. Esperienza, qualifiche e soft skill: possiede tutti i requisiti per avere successo in questa opportunità? Lo scopra qui sotto. The

Novartis

A leading pharmaceutical company in Ivrea is seeking a Qualified Person to independently supervise manufacturing processes and ensure compliance with quality standards. The role involves assessing and releasing manufactured medicinal products, collaborating with various departments, and communicatin

Novartis

A leading pharmaceutical company in Ivrea is seeking a Qualified Person to independently supervise manufacturing processes and ensure compliance with quality standards. The role involves assessing and releasing manufactured medicinal products, collaborating with various departments, and communicatin

Novartis Italia

QA Officer responsible for quality oversight of GMP activities in a sterile production environment, including batch release, documentation, investigations, and audits. Requires a scientific degree and shift work availability.